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rs17145638

From SNPedia

Orientationplus
Stabilizedplus
Make rs17145638(C;C)
Make rs17145638(C;T)
Make rs17145638(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position40026377
is asnp
is mentioned by
dbSNPrs17145638
dbSNP (classic)rs17145638
ClinGenrs17145638
ebirs17145638
HLIrs17145638
Exacrs17145638
Gnomadrs17145638
Varsomers17145638
LitVarrs17145638
Maprs17145638
PheGenIrs17145638
Biobankrs17145638
1000 genomesrs17145638
hgdprs17145638
ensemblrs17145638
geneviewrs17145638
scholarrs17145638
googlers17145638
pharmgkbrs17145638
gwascentralrs17145638
openSNPrs17145638
23andMers17145638
SNPshotrs17145638
SNPdbers17145638
MSV3drs17145638
GWAS Ctlgrs17145638
GMAF0.101
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 23470693OA-icon.png] Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.

GWAS snp
PMID [PMID 23470693OA-icon.png]
Trait Pit-and-Fissure caries
Title Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.
Risk Allele C
P-val 2E-7
Odds Ratio 2.33 [NR] unit decrease